Wireless patient monitoring system and method

ABSTRACT

A method of monitoring a patient includes operating each of one or more wireless sensing devices to measure a physiological parameter from a patient and wirelessly transmit a parameter dataset, and receiving the one or more parameter datasets from the one or more wireless sensing devices. The method further includes calculating a patient condition index based on the one or more parameter datasets, wherein the patient condition index is an indicator of stability of the one or more physiological parameters. A measurement interval is then assigned for each wireless sensing device based on the patient condition index, and each wireless sensing device is operated according to the respective measurement interval.

CROSS REFERENCE TO RELATED APPLICATION

This application is a continuation of U.S. patent application Ser. No.15/041,220, filed Feb. 11, 2016, which is incorporated herein byreference in entirety.

BACKGROUND

The present disclosure relates generally to medical devices and, morespecifically, to medical monitoring devices for monitoring a patient'sphysiology and health status.

In the field of medicine, physicians often desire to monitor multiplephysiological characteristics of their patients. Oftentimes, patientmonitoring involves the use of several separate monitoring devicessimultaneously, such as a pulse oximeter, a blood pressure monitor, aheart monitor, a temperature monitor, etc. Several separate patientmonitoring devices are often connected to a patient, tethering thepatient to multiple bulky bedside devices via physical wiring or cables.Multi-parameter monitors are also available where different sensor setsmay be connected to a single monitor. However, such multi-parametersystems may be even more restrictive than separate monitoring devicesbecause they require all of the sensors attached to a patient to bephysically attached to a single monitor, resulting in multiple wiresrunning across the patient's body. Thus, currently available patientmonitoring devices often inhibit patient movement, requiring a patientto stay in one location or to transport a large monitor with them whenthey move from one place to another.

Further, currently available monitoring devices are often powerintensive and either require being plugged in to a wall outlet orrequire large battery units that have to be replaced and recharged everyfew hours. Thus, monitoring multiple patient parameters is powerintensive and battery replacement is costly in labor and parts. Thus,frequent monitoring is often avoided in order to limit cost and patientdiscomfort, and instead patient parameters are infrequently spotchecked, such as by periodic nurse visits one or a few times a day.While there are some patients that require continuous, real-timemonitoring, such as those patients experiencing a critical healthcondition, the vast majority of patients need only periodic monitoringto check that their condition has not changed. However, patients thatare not being regularly monitored may encounter risky health situationsthat that go undetected for a period of time, such as where rapidchanges occur in physiological parameters that are not checked by aclinician until hours later or until a critical situation occurs.

SUMMARY

The present disclosure generally relates to a patient monitoring systemand method.

A method of monitoring a patient includes operating each of one or morewireless sensing devices to measure a physiological parameter from apatient and wirelessly transmit a parameter dataset, and receiving theone or more parameter datasets from the one or more wireless sensingdevices. The method further includes calculating a patient conditionindex based on the one or more parameter datasets, wherein the patientcondition index is an indicator of stability of the one or morephysiological parameters. A measurement interval is then assigned foreach wireless sensing device based on the patient condition index, andeach wireless sensing device is operated according to the respectivemeasurement interval.

One embodiment of a patient monitoring system includes one or morewireless sensing devices, each wireless sensing device configured tomeasure at least one physiological parameter from a patient andwirelessly transmit a parameter dataset. The system further includes areceiver that receives the parameter dataset from the wireless sensingdevice, a processor, and a monitoring regulation module executable onthe processor. The monitoring regulation module is executable to accessa minimum measurement interval for each of the one or more wirelesssensing devices and process the one or more parameter datasets tocalculate a patient condition index, wherein the patient condition indexis an indicator of stability of the one or more physiologicalparameters. The monitoring regulation module is further executable toassign a measurement interval for each of the one or more wirelesssensing devices based on the patient condition index, wherein themeasurement interval is not less than the minimum measurement intervalfor the respective wireless sensing device. The monitoring regulationmodule is further executable to instruct each of the one or morewireless sensing devices to operate at the respective measurementinterval.

Various other features, objects and advantages of the invention will bemade apparent from the following description taken together with thedrawings.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings illustrate the best mode presently contemplated of carryingout the disclosure. In the drawings:

FIG. 1 provides a schematic diagram of one embodiment of a wirelesspatient monitoring system.

FIG. 2 depicts another embodiment of a wireless patient monitoringsystem.

FIG. 3 depicts one embodiment of a computing system portion of awireless patient monitoring system of the present disclosure.

FIG. 4 depicts one embodiment of a method of monitoring a patient.

FIGS. 5-7A and 7B depict various embodiments of a method of monitoring apatient.

DETAILED DESCRIPTION

The present inventor has recognized that wireless monitoring systems aredesirable for patient comfort, for example to provide more comfort andmobility to the patient being monitored. The patient's movement is notinhibited by wires between sensor devices and/or computing devices thatcollect and process the physiological data from the patient. Thus, smallsensing devices and sensors that can be easily attached to the patient'sbody are desirable, such as sensing devices that are wearable portablecomputing devices. In order to do so, the size of the wireless sensingdevices must be small. The present inventor has recognized that animportant aspect of decreasing the size and weight of wireless sensingdevices is decreasing battery size, and that a weakness in thedevelopment of wireless sensing devices has been power consumption andrequirement for long battery times.

In view of his recognition of problems and challenges in the developmentof wireless sensing devices, the present inventor developed thedisclosed system and method to minimize power consumption of thewireless sensing devices. As provided herein, battery demand for eachwireless sensing device, and thus power requirements for the system as awhole, are decreased by selectively and intelligently operating thewireless sensing devices on an infrequent basis when the patient'scondition is stable and continuous patient monitoring is unnecessary. Inthe patient monitoring method and system disclosed herein, one or morewireless sensing devices are controlled to operate at a measurementinterval that is determined based on a patient condition index thatindicates the stability of one or more physiological parameters measuredfrom the patient by the wireless sensing devices. The measurementinterval may be different for each wireless sensing device depending onthe type of physiological monitoring performed by that device and themedical needs of the patient. For example, a minimum measurementinterval may be set for each wireless sensing device, which may be setbased on patient care standards, patient diagnosis, patient medicalhistory, and/or previous monitoring data for the patient. Moreover, thepatient condition index may be configured to account for healthinformation specific to the patient, such as a diagnosis or a medicalhistory for the patient (e.g., recent medical procedures performed,medication being administered, or the like). Accordingly, the wirelesssensing devices are intelligently controlled to enable maximumcontinuous patient monitoring capabilities when necessary, but can beoperated in a reduced monitoring mode when the patient seems stable inorder to reduce the power requirements of the wireless sensing devicesand increase the battery life of the devices.

Another benefit of the system and method disclosed herein is that thesystem automatically determines when the patient condition hasdeteriorated and automatically initiates continuous monitoring by allwireless sensing devices. Thus, when a clinician responds to an alarmcondition, monitoring data is already available and is continuouslybeing updated for all physiological parameters monitored by the system.This is an improvement over prior art systems, where cliniciansresponding to an alarm condition are required to initiate monitoring byvarious monitoring or sensing devices and wait for those devices toproduce measurements in order to fully assess the patient's condition.

In various embodiments, wireless sensing devices measuring differentphysiological parameters may be networked to a central hub or primarysensing device that determines the patient condition index and themeasurement interval for each of the wireless sensing devices in thenetwork. The hub may communicate with a central, host network, such asof the medical facility. In another embodiment, the wireless sensingdevices may communicate with the host network that calculates thepatient stability index and assigns the measurement intervals. There,the wireless sensing devices may communicate with the host networkdirectly, or indirectly through the hub. For example the hub may serveas an amplifier and/or router for communication between the wirelesssensing devices and the host network.

FIG. 1 depicts one embodiment of a patient monitoring system 1containing five wireless sensing devices 3 a-3 e in wirelesscommunication with a hub 15. The hub 15 is in wireless communicationwith a host network 30 that contains medical records database 33. Forexample, the hub device 15 may be attached to the patient's body, placedon or near the patient's bed, or positioned within range of the patient,such as in the same room as the patient. The hub device 15 may be aseparate, stand alone device, or it may be incorporated and/or housedwith another device within the system 1, such as housed with one of thewireless sensing devices 3 a-3 e. Each wireless sensing device 3 a-3 econtains one or more sensors 9 a-9 e for measuring a physiologicalparameter from a patient, and also includes a base unit 10 a-10 e thatreceives the physiological parameter measurements from the sensors 9 a-9e and transmits a parameter dataset based on those measurements to thehub device 15 via communication link 11 a-11 e. The sensors 9 a-9 e maybe connected to the respective base unit 10 a-10 e by wired or wirelessmeans. The sensors 9 a-9 e may be any sensors, leads, or other devicesavailable in the art for sensing or detecting physiological informationfrom a patient, which may include but are not limited to electrodes,lead wires, or available physiological measurement devices such aspressure sensors, flow sensors, temperature sensors, blood pressurecuffs, pulse oximetry sensors, or the like.

In the depicted embodiment, a first wireless sensing device 3 a is anECG sensing device having sensors 9 a that are ECG electrodes. A secondwireless sensing device 3 b is a non-invasive blood pressure (NIBP)sensing device with a sensor 9 b that is a blood pressure cuff includingpressure sensors. A third wireless sensing device 3 c is a peripheraloxygen saturation (SpO2) monitor having sensor 9 c that is a pulseoximetry sensor, such as a standard pulse oximetry sensor configured forplacement on a patient's fingertip. A fourth wireless sensing device 3 dis a temperature monitor having sensor 9 d that is a temperature sensor.The depicted embodiment of the system 1 further includes a fifthwireless sensing device 3 e that is an EEG monitor having sensors 9 ethat are EEG electrodes. It should be understood that the patientmonitoring system 1 of the present disclosure is not limited to theexamples of sensor devices provided, but may be configured and employedto sense and monitor any clinical parameter. The examples providedherein are for the purposes of demonstrating the invention and shouldnot be considered limiting.

The base units 10 a-10 e of each of the exemplary wireless sensingdevices 3 a-3 e may include analog-to-digital (A/D) converters 13 a-13e, which may be any devices or logic sets capable of digitizing analogphysiological signals recorded by the associated sensors 9 a-9 e. Forexample, the A/D converters 13 a-13 e may be Analog Front End (AFE)devices. The base units 10 a-10 e may further include processors 12 a-12e that receive the digital physiological data from the A/D converters 13a-13 e and create a parameter dataset for transmission to the hub device15 and for the host network 30. Each base unit 10 a-10 e may beconfigured differently depending on the type of wireless sensing device,and may be configured to perform various signal processing functions andor sensor control functions. To provide just a few examples, theprocessor 12 a in the ECG sensing device 3 a may be configured to filterthe digital signal from the ECG sensors 9 a to remove artifact and/or toperform various calculations and determinations based on the recordedcardiac data, such as heart rate, QRS interval, ST-T interval, or thelike. The processor 12 b in the NIBP monitor 3 b may be configured, forexample, to process the physiological data recorded by the sensors 9 bin a blood pressure cuff to calculate systolic, diastolic, and meanblood pressure values for the patient. The processor 12 c of the SpO2sensing device 3 c may be configured to determine a blood oxygenationvalue for the patient based on the digitized signal received from thepulse oximetry sensor 9 c. The processor 12 d of the temperature sensingdevice 3 d may be configured to, for example, determine a temperaturefor the patient, such as a mean temperature based on the digitizedtemperature data received from the thermal sensor 9 d. And the processor12 e of the EEG sensing device 3 e may be configured, for example, todetermine a depth of anesthesia measurement value, such as an entropyvalue or a sedation responsiveness index value.

Accordingly, the processor 12 a-12 e may develop a datasets that, inaddition to the recorded physiological data, also include valuesmeasured and/or calculated from the recorded physiological data. Therespective processors 12 a-12 e may then control a receiver/transmitter5 a-5 e in the relevant wireless sensing device 3 a-3 e to transmitparameter datasets to the hub device 15 via communication link 11 a-11e. The parameter dataset transmitted from the respective wirelesssensing devices 3 a-3 e may include the raw digitized physiologicaldata, filtered digitized physiological data, and/or processed dataindicating information about the respective physiological parametermeasured from the patient.

In other embodiments, the processors 12 a-12 e may not perform anysignal processing tasks and may simply be configured to performnecessary control functions for the respective wireless sensing device 3a-3 e. In such an embodiment, the parameter data set transmitted by therespective processor 12 a-12 e may simply be the digitized raw data ordigitized filter data from the various sensor devices 9 a-9 e.

Each wireless sensing device 3 a-3 e includes a battery 7 a-7 e thatstores energy and powers the various aspects of the wireless monitor.Each processor 12 a-12 e may further include power managementcapabilities, especially where the respective wireless sensing device 3a-3 e contains more demanding electromechanical aspects. Each processor12 a-12 e may monitor a battery status 43 a-43 e (FIG. 3), such as acharge level of the relevant battery 7 a-7 e. The processor 12 a-12 emay communicate the battery status to the hub device 15 by thecommunication link 11 a-11 e. Alternatively or additionally, theprocessor 12 a-12 e may control a local display on the wireless sensingdevice 3 a-3 e to display the battery status 43 a-43 e, and/or maycontrol the emission of an audio and/or visual alert regarding thebattery status 43 a-43 e.

The receiver/transmitter 5 a-5 e of each wireless sensing device 3 a-3 ecommunicates via the respective communication link 11 a-11 e with thereceiver/transmitter 17 of the hub device 15, which may include separatereceiving and transmitting devices or may include an integrated deviceproviding both functions, such as a transceiver. Thereceiver/transmitters 5 a-5 e of the wireless sensing devices 3 a-3 eand the receiver/transmitter 17 of the hub device 15 may be any radiofrequency devices known in the art for wirelessly transmitting databetween two points. In one embodiment, the receiver/transmitters 5 a-5 eand 17 may be body area network (BAN) devices, such as medical body areanetwork (MBAN) devices, that operate as a wireless network. For example,the wireless sensing devices 3 a-3 e may be wearable or portablecomputing devices in communication with a hub device 15 positioned inproximity of the patient. Other examples of radio protocols that couldbe used for this purpose include, but are not limited to, Bluetooth,Bluetooth Low Energy (BLE), ANT, and ZIGBEE.

The hub device may further include computing system 35 having processor19 and memory 21. The hub device 15 may serve to control the wirelesssensing devices 3 a-3 e, and thus may transmit operation commands 45a-45 e (FIG. 3) to the respective wireless sensing devices 3 a-3 e viathe communication link 11 a-11 e to control their monitoring operations.The hub 15 may contain a monitoring regulation module 23 that is a setof software instructions stored in memory and executable on theprocessor to assess the physiological data collected by the wirelesssensing devices 3 a-3 e and determine a patient condition therefrom, andto control the respective wireless sensing devices 3 a-3 e according tothe patient condition.

For example, the monitoring regulation module 23 may process the one ormore parameter datasets 41 a-41 e (FIG. 3) received from the wirelesssensing devices 3 a-3 e to calculate a patient condition index that isan indicator of stability of the one or more physiological parameters.The patient condition index may be any value that indicates a value ofphysiological stability for the patient—i.e. indicating whether themonitored physiological parameters being monitored are in a normal rangefor the patient and remain unchanged for a period of time (stable). Forexample, the patient condition index may be a value on a linear scalebetween stable and critical, such as a scale between 1 and 10, where 1represents that all monitored parameters are in a normal range for thepatient and have been in the normal range for at least a predeterminedamount of time, and 10 represents a critically unstable,life-threatening emergency that requires immediate intervention by aclinician. In an alternative embodiment, the patient condition index maybe a color gradient scale between green, indicating a stable condition,and red, indicating a critically unstable condition. In still otherembodiments, the patient condition index may be any series of valuescapable of being used by the software algorithm to represent the patientcondition as an indicator of stability of one or more of thephysiological parameters being measured by the wireless sensing devices3 a-3 e. As described in further detail herein, the patient conditionindex may be calculated based equally on all monitored parameters, ormay be based more heavily on some subset of the monitored parameters.

The monitoring regulation module 23 then assigns a measurement intervalfor each wireless sensing device based on the patient condition indexand instructs operation of each wireless sensing device 3 a-3 eaccording to the respective measurement interval. For example, a minimummeasurement interval may be stored for each wireless sensing device 3a-3 e and the monitoring regulation module 23 may instruct operation ofeach wireless sensing device 3 a-3 e at its minimum measurement intervalif the patient condition index indicates that all physiologicalparameters being measured from the patient are stable. If the patientcondition index indicates that the patient condition is unstable, themonitoring regulation module 23 may instruct one or more of the wirelesssensing devices 3 a-3 e to increase the monitoring frequency above theminimum measurement interval as appropriate based on the degree ofinstability indicated by the patient condition index. For example, themonitoring regulation module 23 may increase the measurement intervalproportionally to the level of the patient condition index, and mayinstruct any level of monitoring between the minimum measurementinterval for each wireless sensing device and continuous monitoring foreach sensing device depending on the patient condition index. Forexample, if the patient condition index indicates that the physiologicalparameters measured from the patient are unstable and that the patienthas a critical health condition, then the monitoring regulation module23 may instruct continuous monitoring operation of all of the wirelesssensing devices 3 a-3 e.

The hub device 15 may communicate with a host network 30 via a wirelesscommunication link 28, such as to transmit the parameter datasets forthe respective wireless sensing devices 3 a-3 e for storage in thepatient's medical record. The hub 15 has receiver/transmitter 25 thatcommunicates with a receiver/transmitter 31 associated with the hostnetwork 30 on communication link 28, which may operate according to anetwork protocol appropriate for longer-range wireless transmissions,such as on the wireless medical telemetry service (WMTS) spectrum or ona Wi-Fi-compliant wireless local area network (LAN). The host network 30may be, for example, a local computer network having servers housedwithin a medical facility treating the patient, or it may be acloud-based system hosted by a cloud computing provider. The hostnetwork 30 may include a medical records database 33 housing the medicalrecords for the patient, which may be updated to store the parameterdatasets recorded and transmitted by the various wireless sensingdevices 3 a-3 e. The host network 30 may further include other patientcare databases, such as for monitoring, assessing, and storingparticular patient monitoring data. For example, the host network mayinclude an ECG database, such as the MUSE ECG management system producedby General Electric Company of Schenectady, New York.

In various embodiments, the hub device 15 may contain software forprocessing the physiological signals recorded by the various wirelesssensing devices 3 a-3 e. For example, in one embodiment the individualwireless sensing device 3 a-3 e may perform minimal or no signalprocessing on the physiological data measured from the patient, and maysimply transmit the digitized physiological data recorded from therespective sensors 9 a-9 e. Software stored in the hub device 15 maythen be executed on the processor 19 to calculate various usefulparameters from the physiological data, as is explained above withrespect to the exemplary wireless sensing devices 3 a-3 d depicted inFIG. 1. In still other embodiments, minimal or no signal processing maybe performed in the hub device 15, and the hub 15 may simply serve torelay the parameter datasets from the wireless sensing devices 3 a-3 eto the host network 30. In such an embodiment, the computing system 35,including the monitoring regulation module 23, may reside in the hostnetwork 30, as is depicted in the embodiment of FIG. 2.

In the embodiment of FIG. 2, the hub device 15 is omitted and thewireless sensing devices 3 a-3 e communicate directly with the hostnetwork 30. Thus, the receiver/transmitter 5 a-5 e of each wirelesssensing device 3 a-3 e may communicate with a receiver/transmitter 31associated with the host network 30 by the respective communication link11 a-11 e. The communication link 11 a-11 e in this embodiment mayoperate according to any wireless communication protocol listed above.It may be desirable to operate the communication according to a wirelesscommunication protocol that is appropriate for longer-rangetransmission. For example, the wireless sensing devices 3 a-3 e maycommunicate with the host network 30 on the WMTS spectrum or on theWi-Fi spectrum. In such an embodiment, receiver/transmitters 31 may beprovided throughout a patient care facility, such as a hospital, asneeded based on the system configuration and the location of patientsbeing monitored by wireless sensor devices. The host network 30 mayhouse the computing system 35 containing the monitoring regulationmodule 23, and thus the calculation of the patient condition index andmeasurement interval assignment may be conducted by the computing system35 housed in the host network 30. Further, the host network 30 mayprovide one or more central monitoring stations, such as user interfacesat central locations for attending clinicians to monitor patientconditions and/or receive alarm notifications.

FIG. 3 provides a system diagram of an exemplary embodiment of thecomputing system 35 having a monitoring regulation module 23 executableto control the wireless sensing devices 3 a-3 e. The computing system 35includes a processor 19, memory 21, software 37, and communicationinterface 39. The processor 19 loads and executes software 37 frommemory 21, including the monitoring regulation module 23, which is anapplication within the software 37. Each monitoring regulation module 23includes computer-readable instructions that, when executed by thecomputing system 35 (including the processor 19), direct the operationas described in detail herein, including to calculate the patientcondition index and assign the measurement intervals for the wirelesssensing devices 3 a-3 e.

Although the computing system 35 as depicted in FIG. 3 includes onesoftware element 37 encapsulating one monitoring regulation module 23,it should be understood that one or more software elements having one ormore modules may provide the same operation. Similarly, while thedescription provided herein refers to a single computing system 35having a single processor 19, it is to be recognized thatimplementations of such systems can be performed using one or moreprocessors, which may be communicatively connected, and suchimplementations are considered to be within the scope of thedescription. Likewise, the computing system 35 may be implemented asseveral computing systems networked together, including in a cloudcomputing environment. Such an embodiment may be utilized, for example,where the computing system 35 is part of the host network 30.

The memory 21, which includes the medical record database 33, cancomprise any storage media, or group of storage media, readable byprocessor 19 and/or capable of storing software 37. The memory 21 caninclude volatile and non-volatile, removable and non-removable storagemedia implemented in any method or technology for storage ofinformation, such as computer-readable instructions, data structures,program modules, or other data. Memory 21 can be implemented as a singlestorage device but may also be implemented across multiple storagedevices or sub-systems. For example, the software 37 may be stored on aseparate storage device than the medical record database 33. Further, insome embodiments the memory 21 may also store the medical recorddatabase 33, which could also be distributed, and/or implemented acrossone or more storage media or group of storage medias accessible withinthe host network 30. Similarly, medical record database 33 may encompassmultiple different sub-databases at different storage locations and/orcontaining different information which may be stored in differentformats.

Examples of memory devices, or storage media, include random accessmemory, read only memory, magnetic discs, optical discs, flash memory,virtual memory, and non-virtual memory, magnetic sets, magnetic tape,magnetic disc storage or other magnetic storage devices, or any othermedium which can be used to storage the desired information and that maybe accessed by an instruction execution system, as well as anycombination or variation thereof, or any other type of storage medium.Likewise, the storage media may be housed locally with the processor 19,or may be distributed in one or more servers, which may be at multiplelocations and networked, such as in cloud computing applications andsystems. In some implementations, the store media can be anon-transitory storage media. In some implementations, at least aportion of the storage media may be transitory. Memory 21 may furtherinclude additional elements, such a controller capable, of communicatingwith the processor 19.

The communication interface 39 is configured to provide communicationbetween the processor 19 and the various other aspects of the system 1,including the wireless sensing devices 3 a-3 e to receive the parameterdatasets 41 a-41 e and the battery status 43 a-43 e of each respectivedevice 3 a-3 e and to transmit the operation command 45 a-45 e to eachrespective device 3 a-3 e. For example, the communication interface 39may include the receiver/transmitters 17 and 25, and/or thereceiver/transmitter 31 described above with respect to the variousdepicted embodiments.

FIG. 4 depicts one embodiment of a method 80 of monitoring a patient. Atstep 82, a minimum measurement interval is accessed for each of thewireless sensing devices in the system, which in the embodiment depictedin FIG. 4 includes a first monitor and a second monitor. For example,the monitoring regulation module 23 may access a lookup table ordatabase of minimum measurement intervals stored in memory 21 for eachwireless sensing device in the system 1. Alternatively, the minimummeasurement interval may be provided to the system by a clinician, suchas upon system set up. For example the minimum measurement interval maybe a setting established when each wireless sensor device 3 a-3 n(representing any number of wireless sensing devices) is connected tothe system 1. Each of the wireless sensor devices 3 a-3 n is thenoperated at step 84 to measure a physiological parameter from thepatient, and then to transmit a parameter dataset at step 86. Each ofthe parameter data sets is received at step 88, such as by themonitoring regulation module 23.

The monitoring regulation module 23 may further be executed on theprocessor 19 to calculate the patient condition index at step 100. Thepatient condition index may be based equally on all parameter datasetsreceived at step 88. Alternatively, the patient condition indexcalculation may weight one or more of the parameter datasets higher thanthe others. For example, higher weight may be assigned to one or morekey parameter datasets based on at least one of a diagnosis of thepatient, a medical history of the patient, and/or previous parameterdatasets for the patient. For example, the monitoring regulation module23 may receive input from a clinician instructing a key parameter orproviding diagnosis or medical history information that indicates thatcertain physiological parameters are especially important. In stillanother embodiment, the monitoring regulation module 23 may access thepatient's medical records in the medical records database 33 to identifywhether assignment of key parameters is warranted. To provide oneexample, for a patient recovering from a cardiac procedure, ECG may beidentified as a key parameter. Accordingly, the ECG parameter datasetmay be weighed more heavily in the patient condition index than theother datasets. In other words, the patient condition index will be moresensitive to changes in the ECG dataset than in the other datasets.Furthermore, the patient condition index may also account for previousparameter datasets and/or previous patient condition indexes. Forexample, the patient condition index may be sensitive to and reflectabnormal volatility within the parameter datasets, even if the changesremain within the “stable” range. Likewise, if a certain one or more ofthe parameter datasets has an established history of being very stable,changes in that parameter dataset may be weighted more heavily.

The monitoring regulation module 23 may further be executed on theprocessor 19 to assign a measurement interval for each monitor at step110 based on the patient condition index. For example, the monitoringregulation module 23 may access a lookup table that provides theappropriate measurement interval for the associated wireless sensingdevice based on the patient condition index. In another embodiment, themeasurement interval for each monitor may be calculated based on aformula that incorporates the patient condition index. For example, theformula may also account for other factors, such as previous patientcondition index values, previous parameter datasets, etc. At step 111,each of the monitors is operated according to the respective measurementinterval. In certain embodiments, the wireless sensing devices may bepowered down, or turned off, between measurement operations in order tosave battery.

FIGS. 5-7A and 7B depict other embodiments of the method 80 ofmonitoring a patient. In FIG. 5, steps 82-88 are executed for each of anECG monitor, an SpO2 monitor, and an NIBP monitor incorporated in thesystem 1. For the ECG monitor, a minimum measurement interval isaccessed for the ECG monitor at step 82 a, and for the SpO2 monitor atstep 82 b, and for the NIBP monitor at step 82 c. In embodimentscontaining other wireless sensing devices, the steps described hereinare also executed for those monitors. Meanwhile, each respectivewireless sensing device measures a respective physiological parameterand transmits a dataset. The wireless ECG sensing device records ECGdata at step 84 a and transmits the ECG dataset at step 86 a. The ECGdataset is received at step 88 a, such as at the hub device 15 or hostnetwork 30 containing monitoring regulation module 23. Likewise, thewireless SpO2 sensing device measures SpO2 at step 84 b and transmits anSpO2 dataset at step 86 b, which is received at step 88 b. The wirelessNIBP sensing device measures NIBP from the patient at step 84 c, andtransmits an NIBP dataset at step 86 c, which is received at step 88 c.The patient condition index is then calculated and the measurementinterval assigned, which may be executed by various specific methodsteps exemplified in FIGS. 6 and 7A-7B.

In the embodiment of FIG. 6, a parameter index is calculated based onthe parameter dataset from each of the wireless sensing devices. Thepatient condition index is then calculated based on the variousparameter indexes. At step 90 a, an ECG parameter index is calculatedbased on the ECG parameter dataset received at step 88 a. For example,the ECG parameter index may reflect whether the values in the ECGdataset are in the normal range and are stable, such as based onprevious ECG datasets for that patient or based on population normalvalues. At step 92 a, it is determined whether the ECG parameter indexexceeds a threshold indicating that the ECG parameter index is notwithin the stable range. If the threshold is exceeded, then an increasedmeasurement interval may be assigned for the ECG monitor at step 94 a.At step 90 b, an SpO2 parameter index is calculated based on the SpO2dataset received at step 88 b. The system determines at step 92 bwhether a threshold for the SpO2 parameter index is exceeded. If so,then an increased measurement interval is assigned for the SpO2 monitorat step 94 b. At step 90 c, an NIBP parameter index is calculated basedon the NIBP dataset received at step 88 c. If the NIBP parameter indexexceeds a threshold for that index, which is determined at step 92 c,then an increased measurement interval is assigned for the NIBP monitorat step 94 c. In various embodiments, the increased measurement intervalmay reflect the value of the parameter index, such that if the parameterindex indicates that the relevant physiological parameter is at acritical level, then continuous monitoring may be assigned for thatparameter. The increased measurement interval assigned may beproportional to the amount that the relevant threshold is exceeded. Forexample, if all of the parameter indexes indicate that the respectivephysiological parameters are in a critical range, continuous monitoringmay be assigned for each and every wireless sensing device accordingly.

For those wireless sensing devices where the relevant parameter indexdoes not exceed the threshold, a measurement interval still needs to bedetermined, and it is determined based on the patient condition index.In the embodiment depicted in FIG. 6, it is determined at step 98whether a key parameter is indicated. In other words, the systemdetermines whether to calculate the patient condition index basedequally on all of the parameter indexes, or whether certain of theparameter indexes should be weighted more heavily. Such decision may bebased on, for example, a diagnosis or medical history for the patient,such as whether the patient is experiencing a medical condition that islikely to manifest in certain ones of the monitored physiologicalparameters first or to a greater degree than others. If a key parameteris indicated, then the patient condition index is calculated at step 100b based on a formula that weights the key parameter more heavily. Forexample, a set of formulas for calculation of the patient conditionindex may be stored in the memory 21 of the computing system 35 and maybe accessible to the monitoring regulation module, which may determineand access the appropriate formula. If a key parameter is not indicatedat step 98, then the patient condition index is calculated at step 100 abased equally on the parameter indexes.

The measurement interval is then calculated at step 110 based on thepatient condition index. Specifically, the measurement interval iscalculated for each of the wireless sensing devices for which theparameter index threshold was not exceeded at step 92. The wirelesssensing devices are then operated according to each of their respectivemeasurement intervals. For example, wireless sensing devices withmeasurement intervals that are sufficiently long may be turned off atstep 111, and then may be reactivated at the end of the interval inorder to measure the physiological parameter at the prescribed time. Forexample, the monitoring regulation module 23 may send a signal toactivate each respective wireless sensing device at the prescribedmeasurement interval. In other embodiments, the monitoring regulationmodule 23 may provide an instruction of the measurement interval to eachrespective wireless sensing device, which may then each regulatethemselves to measure at that monitoring interval until instructedotherwise.

FIGS. 7A-7B depict another embodiment of a method of monitoring apatient. There, the system checks at step 91 whether the values of therelevant parameter dataset are within a threshold range for that type ofparameter. The threshold may be set according to any method known in theart for assessing patient monitoring data, and may be a patient-specificthreshold range developed based on prior parameter datasets recordedfrom the patient, or may be a population normal threshold rangedeveloped based on a population set relevant to the patient'sdemographic. In the specific example, step 91 a is executed to determinewhether the ECG dataset received at step 88 a contains values that areoutside a threshold range for ECG data. If the ECG dataset is outside ofthe threshold range, then an increased measurement interval is assignedat step 94 a, as is explained above. Likewise, step 91 b is executed todetermine whether the SpO2 dataset received at step 88 b is outside of athreshold range for SpO2 data. If so, then an increased measurementinterval is assigned for the SpO2 monitor at step 94 b Likewise, at step91 c it is determined whether the values in the NIBP dataset received atstep 88 c are outside a threshold range for NIBP data. If so, then anincreased measurement interval is assigned at step 94 c for the NIBPmonitor. As explained above, the increased interval may be proportionalto the amount that the relevant data in the dataset exceeds the relevantthreshold range, and continuous monitoring may be assigned if therelevant dataset is in a critical range. It should be noted that otherembodiments of the method 80 may not execute steps that determine themeasurement intervals separately for the wireless sensing devices basedon the parameter data from that device, and instead all measurementintervals for the wireless sensing devices may be determined andassigned based on the patient condition index.

Assuming that one or more of the datasets received at step 88 are notoutside of a threshold range, step 98 is executed to determine whether akey parameter is indicated. If a key parameter is not indicated, thenthe patient condition index may be calculated based on all of thereceived parameter datasets, with each dataset being weighted equally.Alternatively, the patient condition index may be calculated at step 100d based on any formula stored within the system which may weight keyparameter datasets more heavily than others.

Turning to FIG. 7B, once the patient condition index is calculated, step102 is executed to determine whether the patient condition index exceedsa certain threshold indicating stability. If the patient condition indexindicates that the patient condition is stable, then certain steps maybe executed to minimize battery usage as much as possible. For example,the system may determine whether certain wireless sensing devices may beturned off for an extended period of time, or turned off until thepatient condition worsens or the parameter datasets otherwise indicatethat the eliminated parameter should be resumed. In such an embodiment,certain physiological parameters no longer being monitored may beestimated based on secondary indicia measured from other parametersmeasured by other sensing devices. The method depicted in FIGS. 7A-7Bprovides one such example. Step 103 determines whether SpO2 is a keyparameter, and if not, turns off the SpO2 monitor at step 105. Therespiration rate will then be calculated from the ECG dataset in thenext monitoring cycle, as is indicated by step 107. For example,amplitude modulation of the ECG signal may be used in order to determinerespiration rate, a secondary indicia of SpO2, from the ECG dataset.Thus, the SpO2 monitor may be turned off completely, which conserves thebattery of the SpO2 monitor, meaning that one less battery will need tobe monitored and replaced by clinicians. Further, in certainembodiments, this may also reduce the load on the hub 15 by eliminatingthe demand on the hub to receive the SpO2 dataset from the SpO2 monitorand transmit that dataset to the host network 30.

In other embodiments of the method 80, alternative or additional powerconservation steps may be taken when the patient condition indexindicates patient stability. For example, one or more of the wirelesssensor devices may modify their operation to a low power mode, such asby transmitting a lesser amount of parameter data at a lesser frequency.As another example, the wireless sensor devices may modify their sensingoperation to one that demands less energy. For instance, the wirelessECG sensing device may reduce the number of leads it measures from, suchas by reducing from a 12 lead operation to a 5 lead operation or a 3lead operation.

The minimum measurement interval may then be assigned to the ECG monitorand the NIBP monitor at step 110 b, and at step 111 all of the monitorsmay be turned off until such time as the next measurement is demanded.Returning to step 103, if SpO2 is a key parameter, then the SpO2 monitorwill not be turned off, and instead the minimum measurement intervalwill be assigned to all of the wireless sensing devices.

Such power saving measures exemplified by steps 103-107 would only beexecuted if the patient is stable. If, on the other hand, the patientcondition index indicates at step 102 that a stability threshold isexceeded and thus the patient condition cannot be considered stable,then increased measurement intervals will be assigned accordingly. Forexample, step 104 may be executed to determine how far the patientcondition index is outside of the stable range, such as whether thepatient condition index exceeds a critical threshold. If the criticalthreshold is exceeded, then continuous monitoring may be assigned forall monitors at step 110 d and alarms may be activated at step 112 toalert clinicians to the critical patient condition. If the patientcondition index indicates some instability, but not a critical conditionwarranting an alarm, relative increased measurement intervals may beassigned for the wireless sensing devices so that the patient'scondition can be monitored appropriately.

This written description uses examples to disclose the invention,including the best mode, and also to enable any person skilled in theart to make and use the invention. The patentable scope of the inventionis defined by the claims, and may include other examples that occur tothose skilled in the art. Such other examples are intended to be withinthe scope of the claims if they have structural elements that do notdiffer from the literal language of the claims, or if they includeequivalent structural elements with insubstantial differences from theliteral languages of the claims.

1-20. (canceled)
 21. A patient monitoring system comprising: a firstwireless sensing device configured to measure at least a firstphysiological parameter from a patient and wirelessly transmit a firstparameter dataset based on the first physiological parametermeasurements; a second wireless sensing device configured to measure atleast a second physiological parameter from a patient and wirelesslytransmit a second parameter dataset based on the second physiologicalparameter measurements, wherein the second physiological parameter is adifferent physiological parameter than the first physiologicalparameter; a receiver that receives the first parameter dataset and thesecond parameter dataset; a processor; a monitoring regulation moduleexecutable on the processor to: calculate a patient condition indexbased on the first parameter dataset and the second parameter dataset,wherein the patient condition index is an indicator of stability of thefirst physiological parameter and the second physiological parameter;assign a first measurement interval for the first physiologicalparameter and a second measurement interval for the second physiologicalparameter based on the patient condition index; and operate at least thefirst wireless sensing device to measure the first physiologicalparameter at the first measurement interval.
 22. The patient monitoringsystem of claim 21, wherein the monitoring regulation module is furtherexecutable on the processor to operate the second wireless sensingdevice to measure the second physiological parameter at the secondmeasurement interval, wherein the second measurement interval isdifferent than the first measurement interval.
 23. The patientmonitoring system of claim 21, wherein the monitoring regulation moduleis further executable on the processor to determine that the patient isstable based on the patient condition index, power down the secondwireless sensing device, and then determine a secondary indicia of thesecond physiological parameter based on the first parameter datasetinstead of operating the second wireless sensing device at the secondmeasurement interval.
 24. The patient monitoring system of claim 21,wherein the monitoring regulation module is further executable on theprocessor to calculate the patient condition index by assigning higherweight to one of the first physiological parameter or the secondphysiological parameter.
 25. The patient monitoring system of claim 24,wherein the monitoring regulation module is further executable on theprocessor to select a key parameter based on input from a clinicianidentifying one of the first physiological parameter and the secondphysiological parameter as a key parameter, and then to calculate thepatient condition index by assigning the higher weight to the keyparameter.
 26. The patient monitoring system of claim 24, wherein themonitoring regulation module is further executable on the processor toselect a key parameter based on a diagnosis, a medical history, at leastone and/or previous parameter dataset for the patient, and then tocalculate the patient condition index by assigning the higher weight tothe key parameter.
 27. The patient monitoring system of claim 21,wherein the monitoring regulation module is further executable on theprocessor to calculate a first parameter-specific index for the firstphysiological parameter and a second parameter-specific index for thesecond physiological parameter, and then calculate the patient conditionindex based on the first and second parameter-specific indexes.
 28. Thepatient monitoring system of claim 24, wherein the monitoring regulationmodule is further executable on the processor to calculate the patientcondition index based equally on the first parameter dataset relating tothe first physiological parameter and the second parameter datasetrelating to the second physiological parameter.
 29. The patientmonitoring system of claim 24, wherein the monitoring regulation moduleis further executable on the processor to access a first minimummeasurement interval for the first wireless sensing device and a secondminimum measurement interval from the second wireless sensing device,wherein the first measurement interval is not less than the firstminimum measurement interval and the second measurement interval is notless than the second minimum measurement interval.
 30. A method ofmonitoring a patient, the method comprising: operating a first wirelesssensing device to measure a first physiological parameter from a patientand wirelessly transmit a first parameter dataset based on the firstphysiological parameter measurements; operating a second wirelesssensing device to measure a second physiological parameter from thepatient and wirelessly transmit a second parameter dataset based on thesecond physiological parameter measurements, wherein the secondphysiological parameter is a different physiological parameter than thefirst physiological parameter; receiving the first parameter dataset andthe second parameter dataset at a receiver; calculating a patientcondition index based on the first parameter dataset and the secondparameter dataset, wherein the patient condition index is an indicatorof stability of the first physiological parameter and the secondphysiological parameter; assigning, based on the patient conditionindex, a first measurement interval for the first physiologicalparameter and a second measurement interval for the second physiologicalparameter; and operating at least the first wireless sensing deviceaccording to the first measurement interval.
 31. The method of claim 30,wherein the patient condition index is based equally on both the firstparameter dataset and the second parameter dataset.
 32. The method ofclaim 30, further comprising identifying one of the first physiologicalparameter and the second physiological parameter as a key parameter,wherein calculating the patient condition index includes assigning ahigher weight to parameter datasets associated with the key parameter.33. The method of claim 32, further comprising identifying the keyparameter based on a diagnosis, a medical history, and/or previousparameter datasets for the patient.
 34. The method of claim 30, furthercomprising assigning differing weights to the first parameter datasetand the second parameter dataset, and calculating the patient conditionindex based further on the differing weights.
 35. The method of claim30, further comprising calculating a first parameter-specific index forthe first physiological parameter based on at least the first parameterdata and calculating a second parameter-specific index for the secondphysiological parameter based on at least the second parameter data, andcalculating the patient condition index based on the first and secondparameter-specific indexes.
 36. The method of claim 30, furthercomprising operating the second wireless sensing device to measure thesecond physiological parameter at the second measurement interval,wherein the second measurement interval is different than the firstmeasurement interval.
 37. The method of claim 30, further comprisingdetermining that the patient is stable based on the patient conditionindex, and then determining a secondary indicia of the secondphysiological parameter based on the first parameter dataset instead ofoperating the second wireless sensing device.
 38. The method of claim37, further comprising calculating the patient condition index based onthe first parameter dataset and the second parameter dataset when thesecond wireless sensing device is operating, and determining the patientcondition index based on the first parameter dataset and the secondaryindicia of the second physiological parameter when the second wirelesssensing device is not operating.
 39. The method of claim 38, wherein thefirst physiological parameter is a key parameter, and wherein thepatient condition index assigns higher weight to the first parameterdataset than the second parameter dataset or the secondary indicia ofthe second physiological parameter.
 40. The method of claim 39, furthercomprising operating the second wireless sensing device if at least oneof the first parameter dataset is not within a threshold range, thesecondary indicia is not within a threshold range, and the patientcondition index is not within a threshold range.